Ruihua Zhang, Hilal Daglar, Chun Tang, Penghao Li, Liang Feng, Han Han, Guangcheng Wu, Benjie N. Limketkai, Yong Wu, Shuliang Yang, Aspen X.-Y. Chen, Charlotte L. Stern, Christos D. Malliakas, Randall Q. Snurr, J. Fraser Stoddart
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引用次数: 0
摘要
氢的储存是其应用的关键。开发具有高容积和重力储存能力的吸附材料具有挑战性,而这两种能力对于高效利用氢气作为燃料至关重要。在此,我们报告了氢键有机框架(RP-H100 和 RP-H101)中的受控催化策略,该策略依赖于多个氢键以点接触的方式引导催化,从而产生高体积表面积和重力表面积、坚固性和理想的储氢孔径(~1.2-1.9 nm)。这种方法是将九个咪唑annulated三庚烯六面体组装成一个二级六边形上层结构,该结构包含三个开放通道,其中七个六面体通过这些通道相互渗透,形成一个七重猫式上层结构。RP-H101 在组合温度和压力摆动(77 K/100 bar → 160 K/5 bar)条件下显示出较高的氢气容积输送能力(53.7 g l-1)和重量输送能力(9.3 wt%)。这项工作说明了超分子晶体作为储氢候选材料的优点。
Balancing volumetric and gravimetric capacity for hydrogen in supramolecular crystals
The storage of hydrogen is key to its applications. Developing adsorbent materials with high volumetric and gravimetric storage capacities, both of which are essential for the efficient use of hydrogen as a fuel, is challenging. Here we report a controlled catenation strategy in hydrogen-bonded organic frameworks (RP-H100 and RP-H101) that depends on multiple hydrogen bonds to guide catenation in a point-contact manner, resulting in high volumetric and gravimetric surface areas, robustness and ideal pore diameters (~1.2–1.9 nm) for hydrogen storage. This approach involves assembling nine imidazole-annulated triptycene hexaacids into a secondary hexagonal superstructure containing three open channels through which seven of the hexagons interpenetrate to form a seven-fold catenated superstructure. RP-H101 exhibits high deliverable volumetric (53.7 g l−1) and gravimetric (9.3 wt%) capacities for hydrogen under a combined temperature and pressure swing (77 K/100 bar → 160 K/5 bar). This work illustrates the virtues of supramolecular crystals as promising candidates for hydrogen storage.
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